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Publication numberUS6759469 B2
Publication typeGrant
Application numberUS 10/019,636
PCT numberPCT/JP2001/004010
Publication dateJul 6, 2004
Filing dateMay 15, 2001
Priority dateMay 30, 2000
Fee statusPaid
Also published asDE10192179B3, DE10192179T0, DE10192179T1, DE10197400A5, US20030088013, WO2001092411A1
Publication number019636, 10019636, PCT/2001/4010, PCT/JP/1/004010, PCT/JP/1/04010, PCT/JP/2001/004010, PCT/JP/2001/04010, PCT/JP1/004010, PCT/JP1/04010, PCT/JP1004010, PCT/JP104010, PCT/JP2001/004010, PCT/JP2001/04010, PCT/JP2001004010, PCT/JP200104010, US 6759469 B2, US 6759469B2, US-B2-6759469, US6759469 B2, US6759469B2
InventorsMasashi Kudo, Takashi Amemiya, Arata Iida
Original AssigneeNok Corporation
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Butyl rubber composition
US 6759469 B2
Abstract
A butyl rubber composition, which comprises 100 parts by weight of butyl rubber and 30 to 150 parts be weight of carbon black having a CTAB specific surface area of 30 to 100 m2/g and preferably further contains 10 to 100 parts by weight of a flat filler having an average particle size of 1 to 40 μm and an aspect ratio of 5 or more and 0.05 to 5 parts by weight of a coupling agent of organometallic compound is provided. The butyl rubber composition can give vulcanization molded products capable of effectively sealing a carbon dioxide refrigerant without generation of blisters, etc. therein.
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Claims(16)
What is claimed is:
1. A butyl rubber composition for use as a molding material for sealing of a carbon dioxide refrigerant which comprises 100 parts by weight of butyl rubber and 30 to 150 parts by weight of carbon black having a CTAB (cetyltrimethylammonium bromide) specific surface area of 30 to 100 m2/g.
2. A butyl rubber composition according to claim 1, wherein 10 to 100 parts by weight of a flat filler having an average particle size of 1 to 40 μm and an aspect ratio of 5 or more and 0.05 to 5 parts by weight of a coupling agent of organometallic compound are further contained.
3. A butyl rubber composition according to claim 1 for use as a molding material for use in carbon dioxide.
4. A butyl rubber composition according to claim 3 for use as a molding material for air conditioner sealing materials.
5. A butyl rubber composition according to claim 4 for use as a molding material for air conditioner squeeze packings.
6. A butyl rubber composition according to claim 2 for use as a molding material for use in carbon dioxide.
7. A butyl rubber composition according to claim 6 for use as a molding material for air conditioner sealing materials.
8. A butyl rubber composition according to claim 7 for use as a molding material for air conditioner squeeze packings.
9. A sealing material for a carbon dioxide refrigerant molded from the butyl rubber composition of claim 1.
10. A sealing material according to claim 9, wherein the sealing material is a material for air conditioner seals.
11. A sealing material according to claim 10, wherein the sealing material is a material for air conditioner squeeze packings.
12. A butyl rubber composition formulated so that carbon dioxide is substantially non-soluble in the composition, which butyl rubber composition consists essentially of 100 parts by weight of butyl rubber and 30 to 150 parts by weight of carbon black having a CTAB (cetyltrimethylammonium bromide) specific surface area of 30 to 100 m2/g.
13. A butyl rubber composition according to claim 12, further comprising a filler material.
14. A butyl rubber composition according to claim 13, further comprising an organometallic coupling agent.
15. A butyl rubber composition according to claim 14, further comprising a cross-linking agent.
16. A carbon dioxide resistant sealing element that comprises butyl rubber composition which includes 100 parts by weight of butyl rubber and 30 to 150 parts by weight of carbon black having a CTAB (cetyltrimethylammonium bromide) specific surface area of 30 to 100 m2/g.
Description
TECHNICAL FIELD

The present invention relates to a butyl rubber composition, and more particularly to a butyl rubber composition for effective use as molding materials of sealing materials for air conditioners using carbon dioxide as a refrigerant.

BACKGROUND ART

Heretofore, flon-series gases have been used as air conditioner refrigerants, and it is known that the flon-series gases can destroy global environments due to their chemical structures, for example, by destroying the ozonosphere or by warming the earth's atmosphere. Thus, studies have been extensively made on earth-friendly refrigerants, one of which is carbon dioxide (CO2). CO2 is highly soluble in polymer materials, resulting in permeation into sealing materials or blister generation due to changes in pressure in the use circumstances, etc. It is in the present status that no sealing materials capable of confining CO2 therein have been found yet.

DISCLOSURE OF THE INVENTION

An object of the present invention is to provide a butyl rubber composition capable of giving vulcanization-molded products capable of effectively confining a carbon dioxide refrigerant therein without blister generation.

The object of the present invention can be attained by a butyl rubber composition, which comprises 100 parts by weight of butyl rubber and 30 to 150 parts by weight of carbon black having a CTAB specific surface area (according to ASTM D 3765) of 30 to 100 m2/g. It is preferable that the butyl rubber composition contains 10 to 100 parts by weight of a flat filler having as an average particle size of 1 to 40 μm and an aspect ratio of 5 or more and 0.05 to 5 parts by weight of a coupling agent of organometallic compound.

Butyl rubber is a copolymer of isobutylene and isoprene, where at most 3% by mole of isoprene is copolymerized. In the present invention, it is preferable to use a copolymer containing about 2% by mole of isoprene.

Carbon black having a CTAB (cetyltrimethyl ammonium bromide) specific surface area of 30 to 100 m2/g, preferably 35 to 95 m2/g, is contained in butyl rubber in an amount of 30 to 150 parts by weight, preferably 50 to 130 parts by weight, on the basis of 100 parts by weight of butyl rubber. When carbon black having a CTAB specific surface area of more than 100 m2/g is used, the reinforcing effect is too strong, resulting in increased rubber compound viscosity or dispersion failure, whereas carbon black having a CTAB specific surface area of less than 30 m2/g is used, no practical level reinforcing effect is obtainable and bubbles are formed upon contact with the CO2 refrigerant. This is also true in the case of a lower blending proportion than 30 parts by weight as in the case of a lower CTAB specific surface area of 30 m2/g, whereas in the case of a higher blending proportion than 150 parts by weight, not only kneading will be difficult to conduct due to the resulting increased rubber compound viscosity but also very hard vulcanization molded products will be produced.

When a flat filler is used together with carbon black having such specific surface areas, shieldability against the carbon dioxide refrigerant can be improved. The flat filler includes, for example, clay, mica (mica powder), graphite, molybdenum disulfide, etc., and is used in a proportion of 10 to 100 parts by weight, preferably 30 to 80 parts by weight, to 100 parts by weight of butyl rubber.

The flat filler having an average particle size of 1 to 40 μm, preferably 5 to 30 μm, and an aspect ratio of 5 or more, preferably 10 to 30, can be used. When the average particle size is less than 1 μm or the aspect ratio is less than 5, no improvement of the refrigerant shieldability is observable, whereas when the average particle size is more than 40 μm, not only the practical level reinforcing effect cannot be obtained, but also blister generation appears upon contact with the carbon dioxide refrigerant. When the blending proportion is less than 10 parts by weight, not improvement of the refrigerant shieldability is observable. When the blending proportion is not less than 100 parts by weight, blister generation appears upon contact with the carbon dioxide refrigerant, as in the case where the larger average particle size is used.

In the case of using a flat filler for an improvement of the refrigerant shieldability, it is necessary to use 0.05 to 5 parts by weight, preferably 0.1 to 3 parts by weight, of a coupling agent of organometallic compound at the same time. When the blending proportion is less than 0.05 parts by weight, no coupling effect is observable, and blister generation appears upon contact with the carbon dioxide refrigerant. On the other hand, when the blending proportion is more than 5 parts by weight, cross-linking inhibition appears and the compression set characteristic is deteriorated.

Coupling agent of organometallic compound includes, for example, silane coupling agents such as vinyltrimethoxysilane, vinyltriethoxysilane, vinyl tris(2-methoxyethoxy)silane, vinyl-trichlorosilane, γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropyltriethoxysilane, γ-glycidoxypropylmethyl-diethoxysilane, γ-methacryloxypropyltrimethoxysilane, γ-methacryoloxypropyltri-ethoxysilane, γ-methacryloxypropylmethyldimethoxysilane, γ-methacryoxypropylmethyldiethoxysilane, etc.; titan coupling agents, such as isopropyltriisostearoyl titanate, isopropyltris(dioctylpyrophosphate) titanate, isopropyltri(N-aminoethyl-aminoethyl) titanate, tetraoctyl bis(ditridecylphosphite) titanate, bis(dioctylpyrophosphate) oxyacetate titanate, bis(dioctylpyrophosphate) ethylene titanate, etc.; and aluminum coupling agents such as aluminum ethylate, aluminum isopropylate, aluminum isopropylate mono-sec-butyrate, aluminum sec-butyrate, aluminum alkylacetoacetate diisopropylate, aluminumtrisacetyl acetonate, aluminum alkylacetoacetate, etc., which can be used alone or in cominiation of two or more.

Any of such cross-linking agents as sulfur (donor), morpholine, quinoid, halogenated alkylphenol formaldedhyde resin, etc. can be used, so long as they are applicable to butyl rubber. Butyl rubber composition can contain any other appropriate additives than those mentioned above, for example, a reinforcing agent such as white carbon, etc., a filler such as talc, clay, graphite, calcium silicate, etc., a processing aid such as stearic acid, palmitic acid, paraffin wax, etc., an acid receptor such as zinc oxide, magnesium oxide, etc., an antioxidant, a plasticizer, etc., if desired.

The composition can be prepared by kneading through a mixer such as Intermixer, a kneader, Bambury mixer, etc., or open rolls. Vulcanization thereof can be carried out by heating at about 150° C. to about 200° C. for about 3 to about 60 minutes through an injection molding machine, a compression molding machine, a vulcanization press, etc. Oven vulcanization (secondary vulcanization) can be carried out, if desired, by heating at about 120° to about 200° C. for about 1 to about 24 hours.

BEST MODES FOR CARRYING OUT THE INVENTION

The present invention will be described below, referring to Examples.

EXAMPLES 1

Butyl rubber (Butyl 365, product made by Japan 100 parts by weight
Synthetic Rubber Co., Ltd; isoprene content:
2 mol. %)
Carbon black (CTAB specific surface area:  80 parts by weight
50 m2/g)
Zinc oxide  5 parts by weight
Halogenated alkylphenol formaldehyde resin  5 parts by weight

The foregoing components were kneaded through a kneader and open rolls, and the resulting kneaded product was subjected to press vulcanization at 170° C. for 30 minutes and oven vulcanization (secondary vulcanization) at 140° C. for 10 hours to produce a vulcanized sheet, 150×150×2 mm.

The vulcanized sheet was then subjected to measurement of normal state physical properties according to JIS K-6253 and JIS K-6251 and also to dipping in liquid CO2 at 25° C. for 24 hours, followed by heating at 150° C. for one hour and visual observation of the presence of surface blister generation.

EXAMPLE 2

In Example 1, 70 parts by weight of carbon black having a CTAB specific surface area of 80 m2/g was used as carbon black.

COMPARATIVE EXAMPLE 1

In Example 1, 150 parts by weight of carbon black having a CTAB specific surface area of 10 m2/g was used as carbon black.

COMPARATIVE EXAMPLE 2

In Example 1, 50 parts by weight of carbon black having a CTAB specific surface of 120 m2/g was used as carbon black.

COMPARATIVE EXAMPLE 3

In Example 1, 20 parts by weight of carbon black having a CTAB specific area of 90 m2/g was used as carbon black.

COMPARATIVE EXAMPLE 4

In Example 1, 170 parts by weight of carbon black having a CTAB specific surface area of 30 m2/g was used as carbon black.

Results of measurement and evaluation in the foregoing Examples and Comparative Examples are shown in the following Table 1. In Comparative Examples 2 and 4, kneading itself was found impossible.

TABLE 1
Items of measurement
and evaluation Ex.1 Ex.2 Comp.Ex.1 Comp.Ex.3
[Normal state physical
properties]
Hardness (Durometer A) 81 80 78 60
Tensile strength (MPa) 15.3 16.4 7.3 8.9
Elongation (%) 220 270 210 200
[CO2 resistance]
Presence of blister None None Occurred Occurred
Generation

EXAMPLE 3

Butyl rubber (Butyl 365) 100 parts by weight
Carbon black (CTAB specific surface area:  60 parts by weight
50 m2/g)
Flat, graphite (average particle size: 10 μm;  30 parts by weight
aspect ratio : 20)
γ-Glyidoxypropyltrimethoxysilane  1 parts by weight
Zinc oxide  5 parts by weight
Halogenated alkylphenol formaldehyde resin  5 parts by weight

The foregoing components were subjected to kneading, vulcanization, measurement and evaluation in the same manner as in Example 1. In the measurement, compression set (120° C. for 70 hours) according to JIS K-6262 and CO2 shieldability (70° C.) according to ASTM D-1434 were determined besides the normal state physical properties and CO2 resistance.

EXAMPLE 4

In Example 3, 50 parts by weight of carbon black having a CTAB specific surface area of 80 m2/g was used as carbon black.

EXAMPLE 5

In Example 3, the same amount of flat graphite having an average particle size of 2 μm and an aspect ratio of 10 was used as flat graphite.

EXAMPLE 6

In Example 3, the same amount of isopropyltriisostearoyl titanate was used in place of γ-glycidoxypropyltrimethoxy-silane.

EXAMPLE 7

In Example 3, the same amount of aluminum alkyl acetoacetate was used in place of γ-glycidoxypropyltrimethoxy-silane.

Results of measurement and evaluation in the foregoing Examples 3 to 7 are shown in the following Table 2.

TABLE 2
Items of measurement
and evaluation Ex.3 Ex.4 Ex.5 Ex.6 Ex.7
[Normal state physical properties]
Hardness (Durometer A) 80 81 83 80 80
Tensile strength (MPa) 14.3 15.0 15.1 14.5 14.7
Elongation (%) 260 240 220 260 250
[Compression set]
120° C. for 70 hours (%) 27 26 25 28 27
[CO2 shieldability]
Permeation coefficient 700 750 850 700 700
(cc · mm/m2 · 24 hr · atm)
[CO2 resistance]
Presence of blister none none none none none
Generation

COMPARATIVE EXAMPLE 5

In Example 3, 120 parts by weight of carbon black having a CTAB specific surface area of 10 m2/g was used as carbon black.

COMPARATIVE EXAMPLE 6

In Example 3, 40 parts by weight of carbon black having a CTAB specific surface area of 120 m2/g was used as carbon black.

COMPARATIVE EXAMPLE 7

In Example 3, 15 parts by weight of carbon black having a CTAB specific surface area of 90 m2/g was used as carbon black.

COMPARATIVE EXAMPLE 8

In Example 3, 160 parts by weight of carbon black having a CTAB specific surface area of 30 m2/g was used as carbon black.

COMPARATIVE EXAMPLE 9

In Example 3, the same amount of flat graphite having an average particle size of 0.5 μm and an aspect ratio of 10 was used as flat graphite.

COMPARATIVE EXAMPLE 10

In Example 3, the same amount of flat mica having an average particle size of 50 μm and an aspect ratio of 20 was used in place of the flat graphite.

COMPARATIVE EXAMPLE 11

In Example 3, the same amount of spherical clay having an average particle size of 10 μm and an aspect ratio of 1 was used in place of the flat graphite.

COMPARATIVE EXAMPLE 12

In Example 3, the amount of carbon black and that of flat graphite were changed to 75 parts by weight and 5 parts by weight, respectively.

COMPARATIVE EXAMPLE 13

In Example 3, the amount of carbon black and that of flat graphite were changed to 30 parts by weight and 120 parts by weight, respectively.

COMPARATIVE EXAMPLE 14

In Example 3, no γ-glycidoxypropyltrimethoxysilane was used.

COMPARATIVE EXAMPLE 15

In Example 3, the amount of γ-glycidoxypropyltrimethoxy-silane was changed to 10 parts by weight.

Results of measurement and evaluation in the foregoing Comparative Examples 5 to 15 are shown in the following Table 3. In Comparative Examples 6 and 8, kneading itself was found impossible.

TABLE 3
Items of
measurement Comparative Example No.
and evaluations 5 7 9 10 11 12 13 14 15
[Normal state
physical properties]
Hardness 82 79 81 80 82 81 79 80 77
(Durometer A)
Tensile 8.7 12.4 15.6 13.5 15.1 15.9 6.9 14.5 12.7
strength (MPa)
Elongation(%) 270 290 240 290 270 260 190 280 460
[Compression set]
120° C. for 24 29 26 32 25 21 35 25 68
70 hours (%)
[CO2 Shieldability]
Permeation 600 850 1200 550 1400 1300 350 700 750
Coefficient
(cc · mm/m2 ·
24 hr · atm)
[CO2 resistance]
Presence of blister occurred occurred none occurred none none occurred occurred none
generation

In Examples 1 and 2 and Comparative Examples 1 and 3, the CO2 shieldability (permeation coefficient) was found 1,400, 1,400, 1,200 and 1,600 (cc·mm/m2·24·hr·atm), respectively.

INDUSTRIAL APPLICABILITY

The present butyl rubber composition comprises butyl rubber and carbon black having a specific CTAB specific surface area and can give vulcanization molded products showing a distinguished sealability against carbon dioxide without generation of blisters, etc. against carbon dioxide refrigerant. Particularly, when a flat filler with specific properties and a coupling agent of organometallic compound are contained together, a much better shieldability against the carbon dioxide refrigerant can be obtained.

The present butyl rubber composition showing such distinguished characteristics can be suitably used as molding materials for sealing materials such as O-rings, gaskets, packings, etc. for use in air conditioners, for example, squeeze packings (O-rings, X-rings, D-rings, etc.) or as molding materials for sealing materials for refrigerator oil (polyalkylene glycol, etc.) applicable to a carbon dioxide refrigerant.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US6407166 *Feb 18, 1999Jun 18, 2002Bridgestone CorporationElastomeric compositions for damping
JP2000170656A Title not available
JPH093278A Title not available
JPH0260952A Title not available
JPH04120186A Title not available
JPH05263941A Title not available
JPH06345915A Title not available
JPH11293075A Title not available
JPS62273279A Title not available
WO1997023561A1Dec 25, 1996Dec 25, 1996Asahi Glass Co LtdResin composition for building materials and double-glazed unit
Classifications
U.S. Classification524/495, 524/496, 524/499
International ClassificationC09K3/10, C08K5/56, C08K3/04, C08L23/22, C08K7/00, F25B41/00
Cooperative ClassificationC08L23/22, C09K2200/0208, C09K2200/061, C09K3/10
European ClassificationC09K3/10
Legal Events
DateCodeEventDescription
Dec 7, 2011FPAYFee payment
Year of fee payment: 8
Dec 17, 2007FPAYFee payment
Year of fee payment: 4
Oct 16, 2007CCCertificate of correction
Dec 28, 2001ASAssignment
Owner name: DENSO CORPORATION, JAPAN
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:KUDO, MASASHI;AMEMIYA, TAKASHI;IIDA, ARATA;REEL/FRAME:012705/0051;SIGNING DATES FROM 20011019 TO 20011025
Owner name: NOK CORPORATION, JAPAN
Owner name: NOK CORPORATION 12-15, SHIBADAIMON 1-CHOME, MINATO
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:KUDO, MASASHI /AR;REEL/FRAME:012705/0051;SIGNING DATES FROM 20011019 TO 20011025